Z-0481-2009

Cannabinoids Intercept Micro Plate EIA 100 plate kit

Name: Z-0481-2009 Cannabinoids Intercept Micro Plate EIA 100 plate kit
Creator: OraSure Technologies, Inc.
Published: 2008-09-08
License: https://open.fda.gov/license/

OraSure Technologies, Inc. / initiated 2008-09-08 / Terminated

FDA source

OraSure Technologies, Inc. began a recall of Cannabinoids Intercept Micro Plate EIA 100 plate kit on 2008-09-08. The reason FDA records is "Readings, high: intermittent high absorbance readings. For further information, please contact the firm at 610-882-1820". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0481-2009
Status: Terminated
Initiated: 2008-09-08
Posted: 2008-12-18
Terminated: 2008-12-18
Recalling firm: OraSure Technologies, Inc.
Product: Cannabinoids Intercept Micro Plate EIA 100 plate kit
Product code: LDJ Enzyme Immunoassay, Cannabinoids
Reason for recall: Readings, high: intermittent high absorbance readings. For further information, please contact the firm at 610-882-1820.
FDA root cause: Other
Action: On 9/8/08, the recalling firm telephoned the customer to inform them of the problem. As a follow up to the telephone call, the recalling firm issued a recall letter dated 9/11/08 to the customer.
Quantity in commerce: 1 kit
Distribution: The product was shipped to one customer in New York.
Product codes and lots: Product number 11181C. Lot number 6609532 exp 12/2008

Product code LDJ

K002375Class IIStc Cannabinoids Intercept Micro-Plate Eia, Model 1118IOraSure Technologies, Inc. / cleared 2001-01-26

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)